-
1
-
-
0011939540
-
The genetics and transmissibility of human spongiform encephalopathy
-
Baker HF, Ridley RM. The genetics and transmissibility of human spongiform encephalopathy. Neurodegeneration 1992; 1: 3-16
-
(1992)
Neurodegeneration
, vol.1
, pp. 3-16
-
-
Baker, H.F.1
Ridley, R.M.2
-
2
-
-
0027731067
-
Neuropathology of spongiform encephalopathies in humans
-
Bell JE, Ironside JW. Neuropathology of spongiform encephalopathies in humans. Br Med Bull 1993; 49: 738-77
-
(1993)
Br Med Bull
, vol.49
, pp. 738-777
-
-
Bell, J.E.1
Ironside, J.W.2
-
3
-
-
0028211267
-
Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: A neuropathological study
-
Billette de Villemeur T, Gelottt A, Deslys JP. Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study. Neuropathol Appl Neurobiol 1994; 20: 111-17
-
(1994)
Neuropathol Appl Neurobiol
, vol.20
, pp. 111-117
-
-
Billette De Villemeur, T.1
Gelottt, A.2
Deslys, J.P.3
-
4
-
-
0021998646
-
Creutzfeldt-Jakob disease prion proteins in human brains
-
Bockman JM, Kinsbury DI, McKinkley MP, Bendheim PE, Prusiner SB. Creutzfeldt-Jakob disease prion proteins in human brains. N Engl J Med 1995; 312: 73-8
-
(1995)
N Engl J Med
, vol.312
, pp. 73-78
-
-
Bockman, J.M.1
Kinsbury, D.I.2
McKinkley, M.P.3
Bendheim, P.E.4
Prusiner, S.B.5
-
5
-
-
0022416003
-
Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy
-
Brown P, Gajdusek DC, Gibbs CJ, Asher DM. Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy. N Eng J Med 1985; 313: 728-31
-
(1985)
N Eng J Med
, vol.313
, pp. 728-731
-
-
Brown, P.1
Gajdusek, D.C.2
Gibbs, C.J.3
Asher, D.M.4
-
6
-
-
0025372832
-
A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease
-
Brown P, Wolff A, Gajdusek DC. A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease. Neurology 1990; 40: 887-90
-
(1990)
Neurology
, vol.40
, pp. 887-890
-
-
Brown, P.1
Wolff, A.2
Gajdusek, D.C.3
-
7
-
-
0027531316
-
βPP participates in PrP-amyloid plaques of Gerstmann-Straussler-Scheinker disease. Indiana kindred
-
Bugiani O, Giaccone G, Verga L et al. βPP participates in PrP-amyloid plaques of Gerstmann-Straussler-Scheinker disease. Indiana kindred. J Neuropathol Exp Neurol 1993; 52: 66-70
-
(1993)
J Neuropathol Exp Neurol
, vol.52
, pp. 66-70
-
-
Bugiani, O.1
Giaccone, G.2
Verga, L.3
-
8
-
-
0025330687
-
Prion dementia without characteristic pathology
-
Collinge J, Owen F, Poulter M et al. Prion dementia without characteristic pathology. Lancet 1990; 336: 7-9
-
(1990)
Lancet
, vol.336
, pp. 7-9
-
-
Collinge, J.1
Owen, F.2
Poulter, M.3
-
9
-
-
0026650443
-
Inherited prion disease with 144 base pair gene insertion: 2. Clinical and pathological features
-
Collinge J, Brown J, Hardy J et al. Inherited prion disease with 144 base pair gene insertion: 2. Clinical and pathological features. Brain 1992; 115: 687-710
-
(1992)
Brain
, vol.115
, pp. 687-710
-
-
Collinge, J.1
Brown, J.2
Hardy, J.3
-
11
-
-
0027141709
-
Overview of the transmissible spongiform encephalopathies: Prion protein disorders
-
DeArmond SL. Overview of the transmissible spongiform encephalopathies: prion protein disorders. Br Med Bull 1993; 49: 725-37
-
(1993)
Br Med Bull
, vol.49
, pp. 725-737
-
-
DeArmond, S.L.1
-
12
-
-
0028108709
-
Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease
-
de Silva R, Ironside JW, McCardle L et al. Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease. Neurosci Lett 1994; 179: 50-2
-
(1994)
Neurosci Lett
, vol.179
, pp. 50-52
-
-
De Silva, R.1
Ironside, J.W.2
McCardle, L.3
-
13
-
-
0025967257
-
Scrapie-associated prion protein accumulates in astrocytes during scrapie infection
-
Diedrich JF, Bendheim PE, Kim YS, Carp RI, Haase AT. Scrapie-associated prion protein accumulates in astrocytes during scrapie infection. Proc Nat Acad Sci USA 1991; 88: 375-9
-
(1991)
Proc Nat Acad Sci USA
, vol.88
, pp. 375-379
-
-
Diedrich, J.F.1
Bendheim, P.E.2
Kim, Y.S.3
Carp, R.I.4
Haase, A.T.5
-
14
-
-
0027741445
-
Diversity in the neuropathology of scrapie-like disease in aminals
-
Fraser H. Diversity in the neuropathology of scrapie-like disease in aminals. Br Med Bull 1993; 49: 792-809
-
(1993)
Br Med Bull
, vol.49
, pp. 792-809
-
-
Fraser, H.1
-
15
-
-
0025797632
-
Localisation of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses
-
Guiroy DC, Yanagihara R, Gajdusek DC. Localisation of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses. Acta Neuropathol 1991; 82: 87-92
-
(1991)
Acta Neuropathol
, vol.82
, pp. 87-92
-
-
Guiroy, D.C.1
Yanagihara, R.2
Gajdusek, D.C.3
-
16
-
-
0026692758
-
Immunohistochemical study of kuru plaques using antibodies against synthetic protein peptides
-
Hashimoto K, Mannen T, Nobuyuki N. Immunohistochemical study of kuru plaques using antibodies against synthetic protein peptides. Actn Neuropathol 1992; 83: 613-7
-
(1992)
Actn Neuropathol
, vol.83
, pp. 613-617
-
-
Hashimoto, K.1
Mannen, T.2
Nobuyuki, N.3
-
17
-
-
0028040838
-
Prion protein immunocytochemistry: The development of reliable protocols for the investigation of Creutzfeldt-Jakob disease
-
Hayward PAR, Bell JE, Ironside JW. Prion protein immunocytochemistry: the development of reliable protocols for the investigation of Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol 1994; 20: 375-83
-
(1994)
Neuropathol Appl Neurobiol
, vol.20
, pp. 375-383
-
-
Hayward, P.A.R.1
Bell, J.E.2
Ironside, J.W.3
-
18
-
-
0023390305
-
Methods in laboratory investigation: Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids
-
Kitamoto T, Ogomori K, Tateishi J, Pruisiner SB. Methods in laboratory investigation: formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids. Lab Invest 1987; 57: 230-6
-
(1987)
Lab Invest
, vol.57
, pp. 230-236
-
-
Kitamoto, T.1
Ogomori, K.2
Tateishi, J.3
Pruisiner, S.B.4
-
19
-
-
0026751775
-
Abnormal isoform of prion protein accumulates in the synaptic structures of the CNS in patients with Creutzfeldt-Jakob disease
-
Kitamoto T, Shin R, Doh-Ura K et al. Abnormal isoform of prion protein accumulates in the synaptic structures of the CNS in patients with Creutzfeldt-Jakob disease. Am J Pathol 1992; 140: 1285-94
-
(1992)
Am J Pathol
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.2
Doh-Ura, K.3
-
20
-
-
0023928966
-
Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies
-
Kitamoto T, Tateishi J. Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies. Am J Pathol 1988; 131: 435-43
-
(1988)
Am J Pathol
, vol.131
, pp. 435-443
-
-
Kitamoto, T.1
Tateishi, J.2
-
21
-
-
0026487234
-
Prion protein immunocytochemistry helps to establish the true incidence of prion diseases
-
Lantos PL, McGill IS, Janota I et al. Prion protein immunocytochemistry helps to establish the true incidence of prion diseases. Neurosci Lett 1992; 147: 67-71
-
(1992)
Neurosci Lett
, vol.147
, pp. 67-71
-
-
Lantos, P.L.1
McGill, I.S.2
Janota, I.3
-
22
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
-
Medori R, Tritschler JH, LeBlanc A et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. New Eng J Med 1992; 7: 444-9
-
(1992)
New Eng J Med
, vol.7
, pp. 444-449
-
-
Medori, R.1
Tritschler, J.H.2
LeBlanc, A.3
-
23
-
-
0025219885
-
Immunohistochemistry localisation of prion protein in spongiform encephalopathies and normal brain tissue
-
Piccardo P, Safar J, Ceroni M, Gajdusek DC, Gibbs CJ. Immunohistochemistry localisation of prion protein in spongiform encephalopathies and normal brain tissue. Neurology 1990; 40: 518-22
-
(1990)
Neurology
, vol.40
, pp. 518-522
-
-
Piccardo, P.1
Safar, J.2
Ceroni, M.3
Gajdusek, D.C.4
Gibbs, C.J.5
-
24
-
-
0028928498
-
Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease
-
Pickering-Brown S, Mann DMA, Owen F et al. Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease. Neurosci Lett 1995; 187: 127-9
-
(1995)
Neurosci Lett
, vol.187
, pp. 127-129
-
-
Pickering-Brown, S.1
Mann, D.M.A.2
Owen, F.3
-
25
-
-
0025997111
-
Concomitant Creutzfeldt-Jakob and Alzheimer diseases
-
Powers JM, Liu Y, Hair LS, Kascsack RJ, Lewis LD, Levy LA. Concomitant Creutzfeldt-Jakob and Alzheimer diseases. Acta Neuropathol 1991; 83: 95-8
-
(1991)
Acta Neuropathol
, vol.83
, pp. 95-98
-
-
Powers, J.M.1
Liu, Y.2
Hair, L.S.3
Kascsack, R.J.4
Lewis, L.D.5
Levy, L.A.6
-
26
-
-
0026181912
-
Molecular biology and pathology of scrapie and the prion diseases of humans
-
Prusiner SB, DeArmond SJ. Molecular biology and pathology of scrapie and the prion diseases of humans. Brain Pathol 1991; 1: 297-309
-
(1991)
Brain Pathol
, vol.1
, pp. 297-309
-
-
Prusiner, S.B.1
DeArmond, S.J.2
-
27
-
-
0027741446
-
Developments in diagnosis for prion diseases
-
Tateishi J, Kitamoto T. Developments in diagnosis for prion diseases. Br Med Bull 1993; 49: 971-9
-
(1993)
Br Med Bull
, vol.49
, pp. 971-979
-
-
Tateishi, J.1
Kitamoto, T.2
-
28
-
-
0028878943
-
Inherited prion diseases and transmission to rodents
-
Tateishi J, Kitamoto T. Inherited prion diseases and transmission to rodents. Brain Pathol 1995; 5: 53-9
-
(1995)
Brain Pathol
, vol.5
, pp. 53-59
-
-
Tateishi, J.1
Kitamoto, T.2
-
29
-
-
0022530547
-
Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration
-
Weller RO, Steart PV, Powell-Jackson JD. Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration. Neuropathol Appl Neurobiol 1986; 12: 117-29
-
(1986)
Neuropathol Appl Neurobiol
, vol.12
, pp. 117-129
-
-
Weller, R.O.1
Steart, P.V.2
Powell-Jackson, J.D.3
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